Incidental Mutation 'IGL01760:Eif1ad3'
ID 153257
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Eif1ad3
Ensembl Gene ENSMUSG00000072905
Gene Name eukaryotic translation initiation factor 1A domain containing 3
Synonyms Gm2016
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.463) question?
Stock # IGL01760
Quality Score
Status
Chromosome 12
Chromosomal Location 87840842-87844629 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to T at 87843791 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000105774 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000110147]
AlphaFold Q3TQZ4
Predicted Effect probably benign
Transcript: ENSMUST00000110147
SMART Domains Protein: ENSMUSP00000105774
Gene: ENSMUSG00000072905

DomainStartEndE-ValueType
low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 2.58e-46 SMART
low complexity region 125 144 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre5 T A 8: 84,458,586 (GRCm39) T147S probably benign Het
Chst3 A T 10: 60,022,292 (GRCm39) V185D probably damaging Het
Col14a1 A C 15: 55,286,855 (GRCm39) D892A unknown Het
Dop1a A G 9: 86,401,976 (GRCm39) T1059A probably benign Het
Erlec1 A C 11: 30,884,731 (GRCm39) S441A probably benign Het
Frmd4b G T 6: 97,285,663 (GRCm39) T289N probably damaging Het
Gm6133 G A 18: 78,393,390 (GRCm39) R128Q probably benign Het
Gnai2 A G 9: 107,493,717 (GRCm39) S155P probably damaging Het
Hrob T C 11: 102,146,422 (GRCm39) C233R probably benign Het
Hspg2 T C 4: 137,239,982 (GRCm39) S517P possibly damaging Het
Ighv9-1 C A 12: 114,057,814 (GRCm39) E29* probably null Het
Lrp1 T C 10: 127,409,370 (GRCm39) K1583R probably benign Het
Ltbp1 C T 17: 75,534,145 (GRCm39) T211M probably damaging Het
Mttp A G 3: 137,817,497 (GRCm39) S418P probably benign Het
Napa A G 7: 15,832,669 (GRCm39) N23S possibly damaging Het
Odf2 C A 2: 29,804,472 (GRCm39) Q347K probably damaging Het
Ogdhl A G 14: 32,061,894 (GRCm39) D504G probably damaging Het
Or10aa1 T C 1: 173,870,191 (GRCm39) L225P probably damaging Het
Pdxdc1 A T 16: 13,677,016 (GRCm39) N273K probably damaging Het
Rslcan18 T C 13: 67,262,015 (GRCm39) I11V probably benign Het
Spidr G T 16: 15,730,424 (GRCm39) R664S possibly damaging Het
Tead3 T C 17: 28,552,055 (GRCm39) N385S probably benign Het
Trim13 T A 14: 61,843,172 (GRCm39) N396K probably benign Het
Trp53bp2 C T 1: 182,275,993 (GRCm39) A160V possibly damaging Het
Vmn2r69 A G 7: 85,056,072 (GRCm39) S689P possibly damaging Het
Vmn2r79 A T 7: 86,651,366 (GRCm39) Q255L probably benign Het
Wsb1 T C 11: 79,132,867 (GRCm39) Y276C probably damaging Het
Zfp236 G T 18: 82,639,547 (GRCm39) N1233K probably damaging Het
Other mutations in Eif1ad3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1567:Eif1ad3 UTSW 12 87,843,754 (GRCm39) missense unknown
R4077:Eif1ad3 UTSW 12 87,843,710 (GRCm39) missense possibly damaging 0.94
R4077:Eif1ad3 UTSW 12 87,843,401 (GRCm39) missense unknown
R4078:Eif1ad3 UTSW 12 87,843,401 (GRCm39) missense unknown
R4641:Eif1ad3 UTSW 12 87,843,446 (GRCm39) missense probably damaging 0.97
R6358:Eif1ad3 UTSW 12 87,843,770 (GRCm39) missense unknown
R7852:Eif1ad3 UTSW 12 87,843,742 (GRCm39) missense unknown
R8313:Eif1ad3 UTSW 12 87,843,764 (GRCm39) missense unknown
Z1088:Eif1ad3 UTSW 12 87,843,704 (GRCm39) missense possibly damaging 0.49
Posted On 2014-02-04